NDC 48951-3204 Calendula Thuja

NDC Product Code 48951-3204

NDC 48951-3204-8

Package Description: 120 g in 1 TUBE, WITH APPLICATOR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Calendula Thuja with NDC 48951-3204 is a product labeled by Uriel Pharmacy Inc.. The generic name of Calendula Thuja is . The product's dosage form is and is administered via form.

Labeler Name: Uriel Pharmacy Inc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM ALGINATE (UNII: C269C4G2ZQ)
  • LACTIC ACID (UNII: 33X04XA5AT)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • ROSEMARY OIL (UNII: 8LGU7VM393)
  • SAGE OIL (UNII: U27K0H1H2O)
  • THYME OIL (UNII: 2UK410MY6B)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • CITRUS PARADISI SEED (UNII: 12F08874Y7)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Uriel Pharmacy Inc.
Labeler Code: 48951
Start Marketing Date: 09-01-2009 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Calendula Thuja Product Label Images

Calendula Thuja Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage

Under age 2: Consult a doctor.

Dosage & Administration

Directions: Fill the provided applicator with 2 to 3 grams of gel and apply at bedtime for 14 nights.

Otc - Active Ingredient

Active Ingredients: Calendula 2X, Echinacea (Purple coneflower) 2X, Marjorana (Marjoram) 2X, Lilium tigrinum (Tiger lily) 3X, Thuja (American arborvitae) 3X, Kreosotum (Creosote) 6X, Pulsatilla (Pasqueflower) 6X, Argentum colloidal (Colloidal silver) 7X, Candida albicans (Yeast) 33X Inactive Ingredients: Distilled water, Glycerin, Sodium alginate, Lactic acid, Eucalyptus oil, Rosemary oil, Sage oil, Thyme oil, Potassium sorbate, Grapefruit seed extract

Inactive Ingredient

Inactive Ingredients: Distilled water, Glycerin, Sodium alginate, Lactic acid, Eucalyptus oil, Rosemary oil, Sage oil, Thyme oil, Potassium sorbate, Grapefruit seed extract

Otc - Keep Out Of Reach Of Children

Use: Temporary relief of vaginal itching and irritation.

Warnings

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing consult a doctor before use. Avoid contact with eyes. Do not use if safety seals on box are broken or missing.BEST WHEN USED WITHIN 30 DAYS OF OPENING.

Otc - Questions

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

* Please review the disclaimer below.